Lupus Advocate Shares Why Clinical Trial Participation by People of Color is Critical
Lupus Advocate Shares Why Clinical Trial Participation by People of Color is Critical
May 31, 2018

Member of Lupus Research Alliance Young Leaders group, lupus spokesperson, blogger and champion Shanelle Gabriel shares her experience living with lupus from diagnosis to day-to-day management. Her main message –people of color are under-represented in clinical trials and need to participate so that new treatments can be tested among the people who need them most.

This video is part of a collaboration between the Lupus Research Alliance and the digital health company Antidote to share patient perspectives on clinical research.

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